Canonical Allele Identifier: CA2651722302
Gene: ADAM33 HGNC NCBI

Linked Data

gnomAD v4: 20-3667970-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.3667970T>C , CM000682.2:g.3667970T>C GRCh38
NC_000020.10:g.3648617T>C , CM000682.1:g.3648617T>C GRCh37
NC_000020.9:g.3596617T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000356518.6:c.*993A>G ENSP00000348912.2:n.*993A>G
ENST00000379861.8:c.*993A>G ENSP00000369190.4:n.*993A>G
ENST00000466620.5:n.2996A>G
ENST00000483362.1:n.2358A>G
NM_001282447.2:c.*993A>G NP_001269376.1:n.*993A>G
NM_025220.4:c.*993A>G NP_079496.1:n.*993A>G
NM_153202.3:c.*993A>G NP_694882.1:n.*993A>G